Canonical Allele Identifier: PA2825523968
Gene: ANG HGNC NCBI

Linked Data

ClinVar Variation Id: 807061
ClinVar RCV Id: RCV000995108
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091046.1:p.Leu18Gln
CA7083128
NM_001097577.3:c.53T>A